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We performed experiments to characterize the inducibility of nucleotide excision repair (NER) in Caenorhabditis elegans, and to examine global gene expression in NER-deficient and -proficient strains as well as germline vs. somatic tissues, with and without genotoxic stress. We also carried out experiments to elucidate the importance of NER in the adult life of C. elegans under genotoxin-stressed and control conditions. Adult lifespan was not detectably different between wild-type and NER-deficient xpa-1 nematodes under control conditions. However, exposure to 6 J/m2/day of ultraviolet C radiation (UVC) decreased lifespan in xpa-1 nematodes more than a dose of 100 J/m2/day in wild-type. Similar differential sensitivities were observed for adult size and feeding. Remarkably, global gene expression was nearly identical in young adult wild-type and xpa-1 nematodes, both in control conditions and three hours after exposure to 50 J/m2 UVC. Neither NER genes nor protein activity were detectably inducible in young adults that lacked germ cells and developing embryos (glp-1 strain). However, expression levels of dozens of NER and other DNA damage response genes were much (5 to 30-fold) lower in adults lacking germ cells and developing embryos, suggesting that somatic and post-mitotic cells have a much lower DNA repair ability. Finally, we describe a refinement of our DNA damage assay that allows damage measurement in single nematodes.
Nucleotide excision repair (NER) is responsible for the removal of a wide range of DNA helix-distorting damage, including lesions caused by ultraviolet radiation, important environmental contaminants such as polycyclic aromatic hydrocarbons and mycotoxins, as well as some types of cisplatin-induced and oxidative damage [1,2]. The importance of this pathway is illustrated by the human disorder xeroderma pigmentosum (XP), which is caused by a mutation of one of several NER genes (XPA to XPG) that leads to a markedly (~1000-fold) increased susceptibility to skin cancer and, in some cases, neurological effects [3,4]. Furthermore, NER is very highly conserved and observed in all free-living organisms studied in all three domains of life [5–7]. However, in shorter-lived organisms including mice and Caenorhabditis elegans, very few phenotypes associated with NER deficiency have been observed in unstressed organisms. We therefore chose to study in more detail the phenotype of NER-deficient C. elegans both in control and DNA-damaging environments.
C. elegans is a useful model for DNA damage and repair studies because it is a simple organism sharing many homologs with human DNA damage responsive genes [8–10]. Experiments using C. elegans exposed to ionizing radiation or UV have provided powerful insights into the apoptotic and checkpoint pathways [11–14]. Several studies have focused on C. elegans XPA-1, a homolog of the human XP group A protein . Most researchers have reported few obvious phenotypes in xpa-1 mutants or RNAi-treated nematodes in the absence of stress, except for an increase in germline apoptosis in xpa-1 mutants compared to wild-type animals  and a small increase in mutation accumulation . However, Hyun et al.  reported that the xpa-1 strain had a significantly shorter lifespan under control conditions, in contrast to previous observations [18,19]. After genotoxic stress, in contrast, the xpa-1 phenotype is marked, constituting a striking example of a gene-environment interaction. Following UV exposures, xpa-1 mutants display decreased embryonic survival , lack of inducibility of apoptosis in the germline , larval growth arrest, decreased transcriptional competence, DNA damage-induced mutation accumulation , and reduced adult lifespan . Earlier work with a rad-3 mutant, recently identified as allelic to xpa-1 , also demonstrated ultraviolet C (UVC) sensitivity [20–22].
Previously, we described a quantitative polymerase chain reaction (QPCR)-based assay to quantify DNA damage in the nuclear or mitochondrial genomes of C. elegans . Using the QPCR DNA damage assay, we observed that after exposure to UVC, xpa-1 mutant L1s (first larval stage nematodes) failed to repair nuclear DNA damage after 6 or 24 h. Abolition of repair of UVC damage was also observed in xpa-1 and rad-3 mutants using other assays [17,24]. However, we observed no detectable difference in DNA damage between xpa-1 and wild-type L1s in the absence of UV exposure. Inducibility of NER (or other DNA repair pathways) has not been characterized in C. elegans.
The goal of the current study was to study the expression and function of NER genes in C. elegans under control conditions, and to elucidate the importance of NER in genotoxin-stressed adult somatic tissues. We hypothesized that subtle phenotypic differences would be observed between xpa-1 and wild-type nematodes upon careful observation, and therefore examined lifespan, adult growth, and adult feeding, in the presence and absence of genotoxin exposure (single or daily doses of UVC). Since many previous studies have focused on the consequences of ionizing radiation and UV exposures on the germline of exposed animals (e.g., ), we focused here on the effects of UVC on adult C. elegans. All of these phenotypes were indistinguishable under control conditions, but greatly impaired after UVC. We further employed microarray analysis as a particularly powerful way to test for differences between N2 and xpa-1 nematodes, since it offers the ability to examine mRNA levels of most genes in the nematode genome. We hypothesized that basal global gene expression, or early DNA damage-responsive signaling-related gene expression, would be different in N2 and xpa-1 young adults under control conditions and 3 hours after exposure to 50 J/m2 UVC. Instead, global gene expression was highly similar between N2 and xpa-1 nematodes.
Finally, we carried out experiments to test the inducibility of NER in adult C. elegans, and to address the potentially different responses of germline and somatic cells to UVC damage. For these experiments, we used a glp-1 strain, which is a temperature-sensitive mutant deficient in germline proliferation at 25°C . While we did not find evidence for inducibility of NER in C. elegans, the constitutive levels of expression of most DNA damage response genes were markedly higher in N2 and xpa-1 than the germline (and embryo)-deficient glp-1 young adults. This suggests that transcription of DNA repair genes falls off very dramatically after germ cell differentiation and early embryogenesis in C. elegans.
All strains of C. elegans were obtained from the Caenorhabditis Genetic Center (Minneapolis, MN) and cultured as previously described . Bristol N2 (wild-type) and RB684 (xpa-1) were maintained at 20°C; JK1107 (glp-1) was raised at 25°C to prevent germline proliferation . C. elegans embryos were prepared as previously described to yield age-synchronized adult nematodes .
UV radiation exposures were performed in a CL-1000 Ultraviolet Crosslinker (UVP, Upland, CA, USA) with an emission peak at 254 nm (referred to in this manuscript as 'UVC') as previously described . After exposures, nematodes were rinsed from agar plates and either frozen for QPCR-based DNA damage assays or measured for growth or feeding as described below. Single UVC exposures were administered once, on day 0. Chronic UVC exposures were administered every 24h, beginning on day 0. Sampling of nematodes for growth, feeding, and QPCR receiving chronic UVC exposures was performed every 24h with all remaining nematodes then receiving the next UVC exposure. Nematodes were frozen by dripping pelleted nematodes suspended in about 500 µl K-medium  into liquid nitrogen; frozen pellets were stored at −80°C.
Survival assays were performed at 20°C for N2 and xpa-1 adult lifespans and at 25°C for glp-1 lifespans. One day post-L4 molt was counted as "day 0”. A total of 8–10 replicate plates per treatment group were monitored; four separate (in time) experiments were carried out. Plates had between 26 and 42 non-censored nematodes each. Censored nematodes were those that crawled onto the sides of the petri dishes and dessicated, were lost during transfer, or disappeared but were not observed to be dead. Nematodes were transferred by washing on a daily basis during the first 7–8 days and every 1–3 days thereafter.
Adult nematodes were rinsed from plates, allowed to settle, and the pellet was transferred to the sample cup of a COPAS Biosort  (Union Biometrica Inc., Somerville, MA, USA) and diluted to approximately 1 nematode/µL. The COPAS Biosort was used as previously described to measure the optical extinction of individual nematodes (EXT), which takes into account nematode length as well as optical density (width and opacity) [29,30]. In this manuscript, we use the generic terms “size” to refer to optical extinction and “growth” to refer to age-related increases in EXT. After the nematodes were measured, they were dispensed onto fresh E. coli-seeded agar plates and incubated at 20° C until the following day.
Feeding assays were modified from Boyd et al. . Nematodes were transferred to the sample cup of the COPAS Biosort and diluted to approximately 1 nematode/µL. Twenty-five adults were then dispensed into each well of a 96-well plate, containing a mixture of K-medium and OP50 E. coli at a final volume of 50µL. After 1–4 h, 5 µL aliquots of Fluoresbrite® polychromatic red microspheres (0.5 µm diameter; diluted 1:20 in K-medium) (Polysciences, Inc., Warrington, PA) were pipetted into each well and plates were rotated on a nutator mixer for 5 min. The nematodes were allowed to ingest the microspheres for 10 additional min (15 min total) and were then anesthetized using 5 µL of sodium azide (10 mM, final concentration), inhibiting further bead ingestion. Nematodes were aspirated from each well with the COPAS Biosort ReFLx; the level of red fluorescence for individual C. elegans were measured and referred to as “feeding”.
Dose responses for xpa-1 and N2 were plotted together for single and chronic UVC exposures and at all time points. The dose responses were significantly different (p < 0.05) as indicated by non-overlapping standard error bars (Fig. 3 and Fig.4). The mean responses +/− standard errors for starved wild-type nematodes were included for reference.
Previously, we described the adaptation of a QPCR-based DNA damage assay [32,33] to C. elegans . This assay is based on the ability of DNA damage to block the progression of the DNA polymerase used for PCR amplification. Thus, damaged samples are amplified less well than control samples when the assay is carried out using quantitative conditions. The degree of inhibition of amplification of large (~10 kb) genomic fragments is used to quantify the number of lesions. Small (~200 bp) fragments are also amplified from the mitochondrial and nuclear genomes to permit, respectively, normalization to mitochondrial copy number and verification of equal starting amount of nuclear DNA.
QPCR conditions were the same for these experiments as previously described , with one change and one major improvement. First, we amplified only one large nuclear target: the amplicon including most of the unc-2 gene . Second, rather than extract genomic DNA from batches of several thousand pelleted and frozen nematodes as previously described, we carried out the PCR reactions on digests of a small number of individual nematodes. This procedure is an adaptation of a commonly used approach to PCR genotyping of C. elegans, and allows measurement of damage in a single nematode of any lifestage, corresponding to ~500–1000 cells. Briefly, adult nematodes in a ratio of 1 per 15 µl (or 1 per 10 µl in the case of glp-1 adults, which have significantly less DNA) were added by picking to lysis buffer (1× PCR buffer with proteinase K: using the rTth XL DNA polymerase (XL PCR) kit from Applied Biosystems, add 300 µl of 3.3× PCR buffer, 50 µl of Proteinase K (20 mg/ml; Qiagen), to 650 µl of dH2O). We experimented with adding detergents (per ) but found that they gave variable results and did not in general improve amplification. We also tried adding chitinase, but found that inclusion of chitinase in the lysis buffer nearly completely inhibited the PCR reaction. The nematodes in lysis buffer were immediately frozen and stored at −80°. Prior to QPCR, samples were processed as follows: heat to 65°C for 5 minutes; vortex at high speed for 4–5 seconds; heat for an additional 55 minutes at 65°C; heat to 95°C for 15 minutes to deactivate the Proteinase K; and finally briefly vortex and cool to 4°C. Samples can be stored at least several months at −80°C. At least two QPCR reactions with satisfactory 50% quality controls  were carried out per sample. In addition to permitting measurement of damage in a single nematode, this version of the QPCR assay reduces time (~2 h digestion vs. 1+-day extraction of DNA) and expense.
All DNA damage assays were performed on 3–4 tubes of nematodes (3–6 nematodes/tube) picked from a single plate for each condition (dose, time point, presence/absence of pre-treatment). Values for the separate tubes were averaged to give a single value for each plate, which was considered an “n” of 1. In all cases the total “n” was between 4 and 8 (i.e., 4–8 plates obtained in experiments conducted at different times). The DNA lesion frequency data were compared by analysis of variance followed, when appropriate, by Fisher's Protected Least Significant Difference post hoc analysis.
Young adult (24 h post-vulval crescent L4 stage) N2, xpa-1, and glp-1 nematodes were reared at 25°C and exposed to 50 J/m2 UVC radiation on agar plates without food as described , placed on OP50-seeded plates for 2 h 45 minutes, washed off plates and rinsed with K-medium 3 times (~5 minutes each) by allowing settling, resuspending, settling again, etc. Nematodes were frozen by dripping 3,000–5,000 pelleted nematodes suspended in about 500 µl K-medium into liquid nitrogen, and stored at −80°C. The pellets were ground into fine powder with a liquid nitrogen-cooled mortar and pestle  and RNA was extracted using an RNeasy kit (Qiagen, Valencia, CA, USA). RNA was quantified with a NanoDrop Fluorospectrometer (NanoDrop Technologies, Wilmington, DE, USA) and analyzed for integrity with a BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). These exposures were carried out 4 times, twice in 2007 and twice in 2008, for a total “n” of 4.
Gene expression analysis was conducted using Affymetrix /C. elegans/ GeneChip® arrays (Affymetrix, Santa Clara, CA). For the 2007 samples, 500 pg of total RNA was used to produce biotin-labeled cRNA with the Epicentre Biotechnologies TargetAmp 2-Round aRNA Amplification Kit 2.0 according to manufacturer's protocol, with the exception that 10 µl biotin-UTP was incorporated in place of 3.6 µl unlabeled UTP, and final product was eluted in 25 µl water. For the 2008 samples, 100 ng of total RNA was amplified as directed in the Affymetrix Two-Cycle cDNA Synthesis protocol. 15 µg (Epicentre) or 10 µg (Affymetrix Two-Cycle) of amplified cRNAs were fragmented and hybridized to the array for 16 h at 45°C in a rotating hybridization oven using the Affymetrix Eukaryotic Target Hybridization Controls and protocol. Slides were stained and washed as indicated in the Antibody Amplification Stain for Eukaryotic Targets protocol using the Affymetrix Fluidics Station FS450. Arrays were then scanned with an Affymetrix Scanner 3000 and data was obtained using the GenechipÆ Operating Software (GCOS; Version 1.4.0.036).
Data preprocessing, normalization, and error modeling was performed with Rosetta Resolver® (Gene Expression Analysis System version 220.127.116.11.311) after grouping within-year replicates. The resulting fold-changes and p-values were then used for GOMiner  and Cytoscape [37,38] analyses. For both analyses, we made the following comparisons: control vs UVC-exposed in each strain (three total); all pairwise strain comparisons under control conditions (three total); and all pairwise strain comparisons after UVC exposure (three total). The 2007 and 2008 data were not combined at the transcript level, as there was enough variation associated with the years that averaging them would have led to less rather than more statistical power. Rather, we carried out GO enrichment analysis separately for each year, and then compared the results at the level of altered GO biological processes. This approach has been shown to be an effective way of combining otherwise noisy microarray datasets . Detailed descriptions of GOMiner and Cytoscape analyses are accessible as Supplemental methods. Hierarchical clustering, PCA analysis, and visualization were also carried out using GeneSpring versions 7.3 and GX10 (Agilent). Microarray data have been deposited in the National Center for Biotechnology Information's GEO and are accessible through GEO series accession number GSE15159.
As described above, most other reports have indicated that xpa-1 nematodes appear to have fairly normal phenotypes under control conditions, and our own experience with this strain supports those observations. We carried out several experiments designed to examine the xpa-1 control phenotype in more detail. We measured reproduction, lifespan, heat shock response, and finally global gene expression (via microarray) in xpa-1 nematodes. Median lifespans of control wild-type (N2) and xpa-1 nematodes were not detectably different (Fig. 1; Suppl. Table 1). We also compared the number of offspring from N2 and xpa-1 nematodes, and observed no difference (Suppl. Fig. 1). Sublethal (40°C for 30 minutes) heat shock did not cause detectable DNA damage either immediately or 6 hours after exposure in either N2 or xpa-1, and caused a similar level of developmental delay in both strains (Suppl. Fig. 2).
Lifespan was determined for adult C. elegans exposed daily to 6, 12, 25, 50, or 100 J/m2. Daily exposures were carried out to mimic the chronic exposures to genotoxins that organisms often experience outside of the laboratory environment. Although UVC does not penetrate the earth’s atmosphere, it is a convenient experimental tool that generates nuclear DNA damage that is repaired by the same pathway (NER) as important environmental genotoxins such as polycyclic aromatic hydrocarbons and mycotoxins. All UVC treatments greatly reduced xpa-1 lifespan while only 50 and 100 J/m2 reduced wild-type survival (Fig. 1). Exposure to 6 J/m2 UVC resulted in a greater decrease in lifespan in xpa-1 nematodes than did exposure to 100 J/m2 in wild-type nematodes (Suppl. Table 1).
While conducting lifespan experiments, a number of phenotypes were noted in xpa-1 nematodes (Fig. 2). Unexposed xpa-1 nematodes appeared to be slightly darker and longer than wild-type controls. In contrast, UVC-exposed xpa-1 nematodes exhibited a starved phenotype; they were shorter, thinner, and lighter than unexposed xpa-1 or wild-type nematodes at the same UVC doses. After 3 days of 25 J/m2 UVC, xpa-1 nematodes were observed to also have damaged intestinal and pharyngeal structure along with fluid-filled vacuoles and few, if any, embryos present in the gonad (Fig. 2, xpa-1 C25).
The fact that UVC-exposed xpa-1 nematodes appeared to be smaller than wild-type might suggest that a reduction in feeding would be related to the reduction in lifespan. To confirm the growth differential, we quantified nematode size using a COPAS Biosort to measure optical extinction (EXT) as proxy for adult size (see Methods). Adult wild-type and xpa-1 nematodes were exposed to 0, 6, 12, 25, 50, and 100 J/m2 UVC either once (single UVC exposure) or daily (chronic UVC exposures). Wild-type nematodes were only slightly affected by 6 and 100 J/m2 doses of single UVC exposures, while all chronic exposures led to greater but similar decreases in EXT (Fig. 3, left panels). On the other hand, adult xpa-1 size was decreased in a dose-dependent fashion with all UVC doses leading to lower mean EXT values than controls after single or chronic UVC exposures (Fig. 3, right panels). Because UVC-exposed xpa-1 nematodes appeared starved and actually decreased in size throughout the growth experiment, feeding was also quantified using a Biosort. For feeding, nematodes were exposed to UVC on agar plates and red fluorescent microspheres were used to measure feeding rates (see Methods). The red fluorescence of individual nematodes was then measured with the Biosort and used to estimate feeding levels. Feeding levels in both strains varied between individuals and across experimental days, a trend that agreed with previous measurements of feeding . General decreases in feeding levels with time, but no clear dose effects, were observed in wild-type nematodes (Fig. 4, left panels). Feeding levels were greatly affected in xpa-1 nematodes exposed to single doses greater than 12 J/m2 or any chronic doses of UVC (Fig. 4, right panels). Although some UVC-exposed xpa-1 nematodes ingested less red fluorescent microspheres than those starved over the course of the experiment, all fed nematodes, regardless of strain or UVC dose, were larger than unfed nematodes (Fig. 3). In fact, all unfed nematodes were dead by day 4 of the experiment. From these results, it seems unlikely that decreased growth after UV exposures could be entirely attributed to a lack of feeding.
To compare the genotoxin-induced xpa-1 phenotypes that we observed with levels of DNA damage, we dosed adult C. elegans with UVC either once or daily, as described above. We sampled the exposed nematodes to determine the levels of DNA damage that resulted. 1-day old adult C. elegans were exposed to UVC and then frozen for QPCR immediately on day 0 or after 24 h of recovery. After freezing a portion of the nematodes, the remainder then received a daily UVC exposure. Thus, damage was measured immediately after the first exposure on day one, and immediately prior to subsequent exposures on subsequent days. A dose-dependent increase in lesion frequency was observed from 12–50 J/m2 for all strains: wild-type, glp-1 (a germline-deficient mutant strain used to eliminate the confounding effect of cell division; ), and xpa-1 (Fig. 5). A similar level of DNA damage was observed in all strains at the same UVC dose on day 0. However, the lesion frequency after daily exposure to 50 J/m2 increased between days 1 and 5 most rapidly for xpa-1, followed by glp-1 mutants. Wild-type nematodes showed the least time-dependent increase in DNA damage. The effects of strain, dose, and day were all statistically significant, as were the strain by treatment and strain by day interactions (p < 0.0001 in all cases, 3-factor ANOVA). The difference in damage accumulation between wild-type and glp-1 strains must be attributable to the lack of germ cell replication-dependent dilution of the damage in the wild-type strain, since we did not detect any difference in UV photoproduct repair capacity in wild-type and glp-1 mutants (in starved L1 larvae; ). The time-dependent accumulation of damage in the glp-1 mutants is also consistent with the lack of complete repair after 24 h that we previously observed . The relatively high rate of increase in lesion frequency observed in xpa-1 mutants with chronic UVC exposure is probably attributable both to lack of repair and a decrease in dilution of damage by cell division as egg production was diminished in UVC-dosed xpa-1 mutants (data not shown). However, the small decrease in average damage level observed in the xpa-1 mutants on day 1, and the initially slow increase in damage (days 2–3), is likely explained by dilution of the damage, which is no longer possible by days 4 and 5.
Microarray analysis of global gene expression is a powerful way to detect subtle differences between strains because it allows the comparison of transcript levels of nearly all genes in the genome. We carried out microarray analysis of global gene expression in wild-type and xpa-1 young adults under control conditions and 3 h after exposure to 50 J/m2 UVC. The time point of 3 h was chosen to allow us to detect differential signaling in response to the initial damage, as opposed to the differential signaling that would occur at later times due to the persistence of damage in the xpa-1 but not the wild-type strain. A large portion of the nuclear DNA damage caused by UVC is still present at 3 h post-exposure even in NER-proficient nematodes . However, we observed very few differences between the wild-type and xpa-1 strains under either control or UVC-exposed conditions. Specifically, the only gene that was expressed at a level convincingly higher (~10-fold) in xpa-1 than wild-type under both control and UV conditions is K07G5.3 (data not shown), which is located immediately adjacent to xpa-1 on chromosome I. Other than the xpa-1 gene itself, we detected only three genes expressed at a level convincingly lower (<4-fold) in xpa-1 than wild-type under both control and UV conditions: Y48G8AL.11 (haf-6), and Y19D10A.9 (clec-209) and/or F56A4.2 (data not shown). Y19D10A.9 and F56A4.2 are both represented on the array by two probes that cross-hybridize making it impossible to tell if one or both is lower. Thus, even at the level of global gene expression, there are very few differences between wild-type and NER-deficient nematodes.
We also compared global gene expression in wild-type and xpa-1 to glp-1 young adult nematodes under control conditions and 3 h after exposure to 50 J/m2 UVC. The glp-1 strain was included to allow us to contrast the transcriptomic response in germ cell-deficient versus germ cell-bearing animals. Preliminary histological analysis, carried out to examine overall cell appearance and cell integrity in wild-type and xpa-1 nematodes 3 h post-exposure, did not detect any obvious signs of necrotic cell death (cellular destruction/lysis, cell swelling, excessive vacuolization, or fragmented organelles; data not shown). The microarray experiment was carried out twice in 2007, and twice in 2008, and different amplification and labeling protocols were used for the 2007 and 2008 samples. We refer to differences between the 2007 and 2008 experiments as “year” throughout this manuscript. The effect of “year” was noticeable in our gene expression results (e.g., Fig. 6). This is not surprising since such protocol differences are known to introduce some variability , and has the advantage of making it very likely that the gene expression differences that we observed are real.
As stated above, global gene expression was similar in the wild-type and xpa-1 strains, both with and without UVC exposure. Hierarchical clustering and principal components analysis both showed that the strain differences between wild-type and xpa-1 were less important than UV treatment in distinguishing global gene expression patterns (Fig. 6 and Suppl. Fig. 3). The similarity of these two strains is also evident in Supplemental Table 2, which highlights the small number of genes differentially expressed when comparing wild-type and xpa-1 samples in either control or UVC-exposed conditions. In contrast, global gene expression was highly divergent in the glp-1 strain from either wild-type or xpa-1, in both conditions (Fig. 6 and Suppl. Fig. 3).
A full discussion of the extensive constitutive strain differences between glp-1 and other strains, which presumably largely reflect the differences between germ cells/early embryos and somatic cells, is beyond the scope of this manuscript. However, a subset of the differences is pertinent to the topic of DNA damage response. In keeping with our previous finding of much higher expression of many DNA repair genes in embryos vs. adults , the levels of expression of the great majority (~2/3) of known DNA repair-related genes in wild-type and xpa-1 gravid young adults were much higher than in glp-1 young adults, which under the conditions of this experiment lacked germ cells (Fig. 7 and Suppl. data file 1). These included NER genes as well as genes from all other major DNA repair pathways (base excision repair, double-strand break repair, mismatch repair) and other DNA damage responses (e.g., signaling and translesion synthesis). Nearly all of these genes were expressed at least 2-fold higher in wild-type and xpa-1 than glp-1, and many were at 5–30-fold higher in wild-type and xpa-1. The three exceptions to this trend were akt-2, pme-5, and gei-17, which were ~1.5→3-fold higher in glp-1 young adults than in wild-type or xpa-1. The actual fold differences between somatic and germ/embryonic cells must be larger than these, since our “germ cell” samples (wild-type and xpa-1 vs glp-1 young adults) are diluted by the presence of somatic cells.
Detailed GOMiner and Cytoscape (jActiveModules and BiNGO) analyses of strain-to-strain differences under both UV and control conditions can be found in Supplemental data files 2–5 (GOMiner) and 6–7 (BiNGO).
Our microarray analysis also allowed us to examine the transcriptomic response to UVC in wild-type, xpa-1, and glp-1 young adults. These responses were not identical, but did overlap significantly. Differentially expressed transcripts (defined as absolute fold change value > 1.3, a log ratio p-value < 0.05 by Rosetta Resolver, and a log(10) intensity measurement > −0.4) along with fold-change, p-values and GO annotation are listed for each strain and year in Supplemental data file 8. Hierarchical clustering and principal components analysis carried out using only differentially expressed transcripts again showed that the strain differences between wild-type and xpa-1 were minimal, and the glp-1 samples continued to cluster separately (Suppl. Fig. 4 and Suppl. Fig.5).
To identify with more confidence transcripts that are UVC-regulated in both somatic and germ cells, we identified transcripts that were UVC-regulated (as defined above) in both years in each strain (Suppl. data file 9), and then identified transcripts that were present in at least 2 of those 3 lists, and showed the same direction of change after UVC in all 3 strains. These UVC-regulated genes are presented in Table 1. Many of these genes are potentially associated with a stress response of some sort, including metabolism genes (a cytochrome P450 and several UDG glucuronosyl transferases), metal-responsive genes (cdr-4, numr-1), a p-glycoprotein, a fungus-responsive gene (cnc-4), a number of “downstream of daf” genes (dod-22, dod-24, dod-17), two proteolysis-related genes (rpm-1, cul-6), and two DNA damage-responsive genes (pme-4 and crn-2).
We also searched for transcripts that were differentially regulated by UVC in different strains (all 3 pairwise comparisons for glp-1, wild-type, and xpa-1). Although some such genes could be identified based on our criteria for differential expression (Suppl. Table 2), closer inspection of these genes demonstrated that nearly all were in fact regulated in a similar fashion in all strains, and were only included in this table due to narrowly missing one of our criteria for differential expression in one of the strains. We detected only four genes that were qualitatively UVC-regulated in an apparently strain-specific fashion: T22E5.1 (uncharacterized) was down-regulated, and fipr-26 (F53B6.8, uncharacterized) and hoe-1 (E04A4.4, required for germline proliferation) were up-regulated, by UVC in glp-1 but not wild-type and xpa-1 young adults. Conversely, C31A11.5 (uncharacterized) was not upregulated in glp-1 but was between 3- and 10-fold upregulated in wild-type and xpa-1, respectively. We did not test for quantitatively different regulation (e.g., genes that met our statistical criteria for differential regulation in all strains, but for which the degree of up- or down-regulation was different).
Since our list of UVC-regulated genes based on a minimal 1.3-fold change was relatively short (Table 1), we also carried out a jActiveModules network analysis. This algorithm can identify subnetworks highly enriched in regulated genes even if the fold-changes are not large, since it is based only on p-values . We analyzed the resulting enriched subnetworks for GO enrichment, and identified the following biological processes as containing many genes that are coordinately UVC-regulated by a small amount (usually less than 2-fold), in all strains: ubiquitin-mediated proteolysis, glycolysis, transcription, translation, cell division, gamete generation, molting cycle, chromatin organization/DNA packaging and DNA-dependent DNA replication. As an example, a subnetwork enriched in UVC-regulated genes associated with cell cycle progression and gamete generation is shown in Supplemental Figure 6. In addition, genes involved in transcription, translation, cell division, gamete generation, chromatin organization/DNA packaging and DNA-dependent DNA replication were expressed at significantly (2→10-fold) lower levels in glp-1 than wild-type or xpa-1, while glycolysis genes were slightly higher in glp-1 nematodes. The genes in these processes that were consistently UVC-regulated were generally regulated similarly in all of the strains. DNA repair was identified as an altered biological process in the wild-type, but not xpa-1 or glp-1 dataset. However, close examination of DNA repair-related genes showed that only pme-4 was convincingly UVC-regulated in every strain (Fig. 7 and Suppl. data file 10). BiNGO GO enrichment analyses of jActiveModules results are available as Supplementary data files 11–13. GOMiner analysis of UVC-induced gene lists is not included because in no case did more than 4 differentially expressed genes (defined as fold change > 1.3, log ratio p-value < 0.05 by Rosetta Resolver, and log(10) intensity measurement > −0.4) map to a given GO biological process.
Some DNA repair processes are inducible in some organisms (discussed below); it is not known whether NER or other DNA repair processes are inducible in C. elegans. As described above, our analysis of GO biological processes enriched in up-regulated transcripts after UVC did not detect a strong induction of DNA repair gene transcripts. To test more directly the hypothesis that NER would be inducible in C. elegans, we measured repair of UVC-induced DNA damage after pre-exposure to a low dose of UVC in young adult C. elegans. glp-1 nematodes were raised at 25°C to preclude germline cell proliferation and thus cell division-associated dilution of damaged DNA . Young adults were exposed to 6 J/m2 UVC, and then allowed to recover for 18 h prior to a subsequent exposure to 0, 6, 12, 25, 50, or 100 J/m2. Subsets were then frozen at 0, 6, 12, 24, 48, and 72 h post-exposure in order to test the hypothesis that the pre-exposure to UVC would result in faster repair. We did not find strong evidence for inducibility of repair under these conditions (Fig. 8). The main effect of pre-treatment was not significant (p = 0.30). While there appeared to be a trend towards increased repair at 25 and 50 J/m2, we could not carry out specific post-hoc comparisons because neither the interaction of pretreatment with dose nor that of pretreatment with time point and dose were significant (p = 0.15 and 0.66, respectively) (3-factor ANOVA on dose, time point, and presence/absence of pretreatment).
There have been mixed reports on the effects of mutations in the xpa-1 gene on lifespan in C. elegans strains. Hyun et al.  recently reported a markedly shorter lifespan both for the ok698 deletion allele of xpa-1 (used in the current report) and for RNAi-based knockdown of XPA-1. On the other hand, previous reports using both xpa-1(ok698) and rad-3(mn157), a strain carrying an independently isolated deletion mutation of xpa-1 [19,20], detected no difference [18,19]. In these experiments, we detected no difference in lifespan under control conditions.
However, our results are in agreement with those of Hyun et al.  with respect to the dramatic decrease in lifespan in xpa-1 nematodes following adult UVC exposure. We further demonstrate that adult growth and feeding are exquisitely sensitive to UVC damage in the context of NER deficiency, and that these phenotypes are associated with a dramatic increase in DNA damage accumulation. Our lowest dose of UVC (6 J/m2), led to as much or more reduction in lifespan, growth, and feeding in xpa-1 nematodes as did our highest dose (100 J/m2) in wild-type animals. The lack of growth in adults could be due to decreased feeding resulting from a loss in transcriptional competence , or DNA damage-mediated inhibition of endoreduplication upon which adult growth is dependent . We found that feeding was strongly inhibited in UVC-exposed xpa-1 young adults, although it cannot have been completely abolished since starved young adults do not survive past 3 days.
Even using microarray detection of global gene expression, we detected very few differences between the wild-type and xpa-1 strains. K07G5.3, which is located immediately adjacent to xpa-1 on chromosome I, was the gene that was most convincingly differentially expressed, and seems most likely to reflect dysregulation due to the xpa-1 mutation. Similarly, while there was a clear transcriptional response to UVC in all strains, there were also few differences between wild-type and xpa-1 nematodes in that response, suggesting that immediate damage-induced signaling is not dramatically altered in xpa-1 nematodes. We deliberately chose an early time point to avoid detecting transcriptomic differences resulting from the greater persistence of DNA damage in xpa-1 nematodes; a significant amount of UVC-induced DNA damage persists at three hours even in NER-proficient nematodes . These results suggest that the dramatic gene-environment interactions observed in xpa-1 nematodes can be attributed to the persistence of DNA damage in this strain, rather than to differential signaling mediated by xpa-1 under control conditions. It is also possible, however, that the UVC-induced xpa-1 phenotypes result from altered signaling at a different time point, or non-transcriptionally-mediated signaling.
Our results show that not just lifespan, but adult growth, feeding, heat shock resistance, egg production, and even global gene expression in xpa-1 nematodes are nearly identical to wild-type under control conditions. Thus, the level of background DNA damage that occurs in nematodes grown under our laboratory conditions is low enough that no phenotype could be detected using these measures. This suggests that the selective pressure that maintains NER in this short-lived organism must result from genotoxic stressors not encountered under controlled laboratory conditions, or require multiple generations to be evident.
The inducibility of DNA repair is important to characterize in C. elegans given the increasing use of this species for studies of DNA damage and repair. NER is inducible in bacteria and yeast [42–47], but inducibility of NER proteins or repair kinetics appears to be less robust and possibly species-specific in higher eukaryotes [48,49]. This raises the important question of whether C. elegans, a simple eukaryote, is more like the very simple eukaryote yeast, or more like the higher eukaryotes for which it is often used as a model, with respect to DNA damage inducibility. We detected the induction of very few DNA repair genes, and in fact very few DNA damage-responsive genes in general three hours post-UVC exposure, although DNA repair genes are induced by 1–3h in yeast [50,51]. This lack of induction of DNA repair genes was observed both in germ cell- and embryo-containing young adults (wild-type and xpa-1 strains) and in young adults composed entirely of terminally differentiated somatic cells (glp-1 strain). Consistent with these results, Greiss et al.  also detected induction of almost no DNA repair-related genes in C. elegans exposed to ionizing radiation. Furthermore, although induction of some DNA repair genes is p53-dependent in mammals, Derry et al.  detected no genes that were UVC-induced in a cep-1 (C. elegans p53)-dependent fashion.
Since it is possible that our microarray experiment missed an important time point for the detection of transcriptional regulation, or that NER might be inducible through non-transcriptional mechanisms, we also directly tested repair kinetics, but observed no induction. There are caveats associated with this observation. First, we measured repair in both strands of a transcribed gene, rather than specific repair of either transcribed or non-transcribed regions of the genome. Thus, if only transcription-coupled or global genomic repair were induced , it is possible that such a signal would be undetectable. Second, we did not measure repair in germ cells or early embryos, which have much higher levels of DNA repair gene expression (this manuscript and ). The question of whether DNA repair is faster and/or more inducible at earlier lifestages is an important one that should be addressed in future work. Finally, it is conceivable that a different pre-exposure dose might be more effective.
The lifestage-dependent difference in expression of DNA repair as well as other DNA damage-responsive genes is dramatic. Transcription of a high proportion of the components of the DNA damage response is much lower in glp-1 than in gravid wild-type or xpa-1 young adults, despite the dilution of the germ cells/early embryos by somatic cells. Interestingly, one exception to this pattern was genes involved in nonhomologous end-joining, of which only one was higher in germ cell-containing nematodes (cku-80, ~3.5-fold higher). This is consistent with a previous study that found that nonhomologous end-joining is important in non-cycling somatic cells . While our experiments cannot distinguish between germs cells and early embryos, such experiments would be interesting given the fact that cell cycle checkpoint activation is silenced in C. elegans in early embryos, but not in the germline . Importantly, we previously showed that there was no detectable difference in UVC damage repair kinetics between wild-type and glp-1 nematodes when measured in starved L1s, prior to germ cell proliferation .
It would appear that under normal conditions, DNA damage-responsive proteins are present at sufficient levels in adult somatic cells to carry out their functions, as evidenced by the fact that UVC damage is repaired in adults , and checkpoint proteins function in adult somatic cells [54,55]. However, it is possible that levels become insufficient with time, as suggested by our observation of decreased repair in older adults . This insufficiency might be exacerbated by stressful environmental conditions (e.g., exposure to genotoxins), and is particularly interesting in the context of the observation by Weidhaas et al.  that checkpoint proteins, best known for conferring susceptibility to DNA damage-induced apoptotic cell death in germ cells, also confer resistance to DNA damage-induced necrotic cell death in somatic cells.
NER was not detectably inducible by UVC in C. elegans, but germ cells and/or early embryos have a much higher level of expression of NER and other DNA damage response-related genes than do adults consisting only of terminally differentiated somatic cells. NER-deficient C. elegans were nearly indistinguishable from the wild-type strain, even after examination of global gene expression, under control conditions. However, the need for NER in this organism is demonstrated by the dramatic reduction in lifespan, growth, and feeding after low levels of DNA damage. NER deficiency in C. elegans, as in humans, constitutes a dramatic example of a gene-environment interaction.
We thank Julie Rice and Daniel Snyder for technical assistance with COPAS Biosort experiments and C. elegans maintenance, Danica Ducharme of the NIEHS microarray facility for microarray work, and Marjolein Smith for statistical analysis of growth and feeding data. This work was supported by National Institutes of Health [P42 ES10356 to J.M.]; the National Toxicology Program [to W.B.]; and the Intramural Research Program of the National Institute of Environmental Health Sciences [to J.F.]. All nematode strains used in this work were provided by the Caenorhabditis Genetics Center, which is funded by the National Center for Research Resources.
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Conflict of interest
The authors declare that there are no conflicts of interest.